MODIFICATIONS TO SERIES OF CARDIAC CATHETERS

MODIFICATIONS TO SERIES OF CARDIAC CATHETERS is an FDA 510(k)-cleared medical device (K913042) manufactured by Sentron, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 20, 1992. Regulation: 8.